US6004819A - Blood testing device - Google Patents
Blood testing device Download PDFInfo
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- US6004819A US6004819A US09/078,506 US7850698A US6004819A US 6004819 A US6004819 A US 6004819A US 7850698 A US7850698 A US 7850698A US 6004819 A US6004819 A US 6004819A
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- blood
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/483—Physical analysis of biological material
- G01N33/487—Physical analysis of biological material of liquid biological material
- G01N33/49—Blood
- G01N33/4905—Determining clotting time of blood
Definitions
- This invention relates to the measurement of various haemostatis, clotting., and the like properties of blood, and specifically to apparatus enabling measurements of such quantities to be made on blood.
- a device of this kind is disclosed in European Patent Specification No. 129425.
- apparatus for the investigation of blood comprising a columnar reservoir for holding the blood, an elongate tube leading from the reservoir to a waste blood holding vessel, and means for introducing into the reservoir a fluid immiscible with blood to displace the blood through the tube, while simultaneously stirring the blood in the columnar reservoir (hereinafter referred to as "apparatus of the type described").
- apparatus of the type described includes a pair of parallel channels, each channel comprising a columnar reservoir, elongate tube, waste blood holding vessel, and means for introducing a displacing fluid, as described above.
- each channel has a punching station, at which, as disclosed in European Patent Specification No. 129425, a through-hole is punched through the elongate tube, to simulate bleeding. So that the size of the holes in the two tubes is exactly the same, both holes may be punched by a single parallel-sided punching needle. In an alternative embodiment, two exactly similar needles may be provided at corresponding places in the tubes of the two channels.
- the columnar reservoir of both channels is filled with native blood, and caused to flow through the respective elongate tube, by displacement. Both channels are pierced, and the time take for haemostatis to occur (i.e. the formation of a platelet plug in the two holes) is measured in both channels. Because the test is carried out in both channels using whole blood, the platelet plug formed simulates very closely platelet plugs formed in arterial bleeding.
- An anticoagulant agent is then introduced in to the blood flowing in one of the channels. This prevents the blood flowing in that channel from clotting, so that thrombolysis of the platelet plug in that channel can be investigated but does not interfere with the haemostatic plug formation because the haemostatic plug has already been formed when the anticoagulant is introduced.
- a preferred anticoagulant is heparin, because of its low interference with the thrombolytic process.
- the blood in the channel which is not anticoagulated will clot, and this can be measured by appropriate pressure transducers.
- the platelet plug will eventually dissolve, and therefore thrombolysis time can be measured.
- the two-channel instrument of the first embodiment of the present invention is also useful in other clinical diagnostic techniques, for example to determine the effects of various pharmaceuticals substances on clotting, haemostatis and thrombolysis.
- Native blood containing saline control
- identical blood containing the pharmaceutical substance to be investigated in the other and thus the effect on the various properties of the blood can be monitored under closely controlled conditions.
- the invention is concerned with the effect of various substances, for example collagen, on haemostasis/thrombosis.
- a small piece of collagen such as a piece of a surgical suture, may be placed within the elongate tube leading from the columnar reservoir to the blood holding vessel of apparatus of the type described, and the blood caused to flow over the substance.
- the mechanism of platelet thrombus formation on the surface of substances such as collagen is similar to that which occurs during the normal passage of blood through injured blood vessels in the body. Collagen fibres are exposed when blood vessels are ruptured and it is of considerable clinical interest to investigate in detail the effect of collagen during thrombus formation.
- a piece of the substance such as collagen is provided in the elongate tube of the apparatus, and the progress of thrombus formation is followed by observing blood flow in the tube, for example by the measurement of pressure, as disclosed hereinafter, as the formation of a thrombus on the substance causes a characteristic pattern of occlusion of the tube.
- three parallel channels may be provided, to enable the effect of substances such as collagen on thrombus formation to be determined, whilst other measurements are also being performed, for example haemostatis and blood clotting measurements.
- a fourth aspect of the invention relates to the method by which blood flow in apparatus of the type described is measured and controlled.
- a pressure transducer is utilised, to measure variation of pressure in the blood, as the holes are punched, and subsequently occluded by platelet plugs.
- the pressure transducer however is positioned upstream of the punching station, so that the only measurement possible with regarding to clotting in the tube is the point at which blood flow in the tubes ceases completely.
- apparatus of the type described includes a pressure transducer downstream of the elongate tube, and preferably disposed so as to measure pressure in the waste blood holding vessel, whereby the process of blood clotting can be followed.
- the waste holding vessel is; in this embodiment, filled with a fluid immiscible with the blood, which is displaced by the entry of the blood.
- a fifth aspect of the invention is concerned with the mechanism for causing the blood to pass through the elongate tube.
- the blood is displaced by a fluid immiscible therewith, for example paraffin oil, which is supplied to the columnar container using a syringe pump.
- a fluid immiscible therewith for example paraffin oil
- apparatus of the type described includes means for introducing the immiscible fluid into the columnar container, comprising a pressurisable vessel for the immiscible fluid, means for applying a constant pressure head to the pressurisable container, and a capillary tube leading from the pressurisable vessel to the columnar container, the capillary tube having a resistance to flow substantially greater than that of the tube leading from the columnar container to the waste blood holding vessel.
- a seventh aspect of the invention relates to the nature of the columnar container itself.
- the columnar container is essentially a tube provided with a fluid inlet and a fluid outlet at its bottom part, for, respectively, introduction of the displacing fluid, and the outflow of blood.
- One disadvantage of this arrangement is that it necessitates transfer of the blood from one container to another, after it has been taken from the patient, and this can result in the initiation of the clotting process.
- the tube arrangement includes a number of sharp corners over which the blood must flow, and these and the turbulence caused also can initiate the clotting/haemostasis process.
- the columnar container is preferably a plastics syringe, which can be used to take a blood sample from a patient in the ordinary way, and from which the hypodermic needle can then be removed, so that the elongate tube leading to the waste blood holding vessel can be attached.
- the apparatus preferably includes a mounting block for the syringe, which may include temperature control means, for example a water jacket, or a thermostatically controlled heating element.
- the mounting block will generally be adapted for mounting a syringe for each channel.
- the support block may also preferably comprise a port or septum, so that a hypodermic needle may be introduced into the syringe, through its wall, for introduction of the displacement fluid.
- the displacement fluid will normally be less dense than blood, and accordingly the port is preferably positioned close to the bottom of the hypodermic syringe, so that introduction of the displacement fluid causes effective stirring of the blood.
- the elongate tube leading from the syringe to the waste blood vessel is preferably attached by a LUER-type fitting, and by this method virtually all parts of the apparatus which come into contact with blood are rendered disposable. Thus, the syringe, tubing and waste blood holding vessel may all be discarded after use.
- thrombolysis is concerned with the investigation of thrombolysis.
- haemostatis and clotting are relatively quick to occur, thrombolysis will generally require a much longer time for completion, for example from fifteen to forty minutes. If the blood is caused to flow in the elongate tube for the whole of this period, substantial quantities of blood are required. However, once the anticoagulant has been added, it is no longer necessary for the flow of blood to be maintained in the tube, provided that the pressure of the blood remains constant.
- a valve for example a needle valve, for closing the outlet of the waste blood holding vessel, so that after anticoagulated blood has passed through the whole of the elongate tube, the valve can be closed, such that pressure in the system can be maintained, without the loss of blood therefrom.
- the progress of thrombolysis can then be measured, as above, using a pressure transducer in the waste blood holding vessel.
- This arrangement is particularly advantageously used with the arrangement described above of a pressurised vessel for driving the displacement fluid in the columnar blood container.
- means may be provided for reducing the pressure applied to the pressurisable vessel, when the valve is closed.
- the internal pressure in the blood-containing parts of the system (the columnar container, elongate tube and waste blood holding vessel) is substantially below that in the pressurisable container, closing of the valve would result in the overall rise in pressure in the system, because of equalisation of the pressure in the blood-containing parts, and the displacement fluid containing parts.
- means are preferably provided for applying a reduced pressure to the displacement fluid, after closure of the valve.
- the means for applying the reduced pressure may take the form of two pressurisable containers, pressurised to different pressures, and alternatively switchable to provide the pressure to drive the displacement fluid.
- FIG. 1 is a schematic diagram showing one channel of a two-channel blood analysis device
- FIG. 2 is a schematic diagram of the punching station of a two-channel device
- FIG. 3 shows a preferred pressurised vessel arrangement
- FIG. 4 shows samples of haemostatis, clotting, and thrombolysis traces obtained with the instrument of FIGS. 1 and 2, and
- FIGS. 5A and 5B illustrate the investigation of platelet, collagen interaction.
- one channel of a two-channel instrument comprises a columnar container for holding blood, in the form of a 2 ml hypodermic syringe 1, made of a disposable plastics material.
- a elongate polyethylene tube having an internal. diameter of 0.5 mm, and a length of approximately 30 cm is connected to the syringe 1 by means of LUER-type connector 3.
- the tube 2 is inserted through a pressure-tight rubber seal 4 in a waste blood holding vessel 5.
- the waste blood holding vessel 5 is filled with paraffin oil 6, and the level of blood 7 in the vessel rises during the investigation.
- the syringe 1 is received in a syringe mounting block 8, provided with an electrical heating element and thermostat (not shown) to maintain the heating block 8 at a constant temperature of 37° C.
- the plunger 9 of the syringe 1 is secured by a lock (not shown), to prevent its backward movement, on pressurisation of the blood in the syringe.
- the polyethylene tube 2 is threaded through a punching station, generally of the kind described in European Patent Specifiction No. 129425, except for the modification that support is provided for two such polyethylene tubes, and a punching needle 10 is of a sufficient length, and has sufficient movement, to punch through both sides of the tubes 2 of two channels. This is illustrated more clearly in FIG. 2.
- Needle 10 is attached to a plunger 11, which may be manually actuated, but is preferably actuated by means of a solenoid, or hydraulic or pneumatic actuator.
- the shank of the punching needle 10 has a diameter of 0.15 mm.
- Means are provided for enabling the supply of warm saline solution to the punching station, surrounding the tubes, to wash away the blood, as simulated bleeding occurs from holes 12 when the tube is punched.
- An outlet is provided for the saline solution, and means are provided associated with outlet for causing the saline solution to flow between a light-emitting diode, emitting green light, and a silicon photodiode.
- the waste blood holding vessel 5 has three parts, a base 5a, a central tubular part 5b and an upper part 5c.
- the upper 5c has an opening 19 to which is affixed a pressure transducer 20.
- An outlet 21 for paraffin oil is also provided in the upper part 5c.
- a valve 22 is provided for closing outlet 21 from the vessel 5.
- Parts 5a, 5b and 5c of the vessel 5 are assembled as a push-fit, and are sealed by "O" rings 24 and 25.
- FIG. 3 illustrates schematically an arrangement for supplying an immiscible fluid (paraffin oil) under pressure to the two channels of the instrument.
- an immiscible fluid paraffin oil
- the apparatus for FIG. 3 includes two pressurisable vessels 30 and 31, and a three-way tap 32.
- the three-way tap 32 is connected to a low pressure gas supply line 33, and a high pressure gas supply line 34.
- the pressure in line 33 is arranged to be 60 torr, and that in line 34, 360 torr (all pressures referred to herein are gauge pressures) regulators 35 and 36 respectively are provided to maintain the pressure in lines 33 and 34 of the desired level.
- the three-way valve 32 can be turned between a first position, as shown, in which pressure line 33 is connected directly to pressure vessel 30, via line 38, and pressure line 34 is connected directly to vessel 31, via line 39, and a second position, in which pressure line 34 is connected to both pressure vessels 30 and 31.
- Each of vessel 30 and 31 is filled with paraffin oil, and is provided with a respective capillary tube 40, 41 having an internal diameter of approximately 0.18 mm, and a length of approximately 30 cm, to hypodermic needles 42 and 43 respectively.
- Means 46 are provided for applying gas under pressure to both pressure regulators 35 and 36.
- the means 46 may be a pump, or a cylinder of pressurised gas.
- two blood samples are taken from the patient using respective syringes 1 of the two-channels of the apparatus.
- the syringes 1 are placed in the heating block 8 of the apparatus, and the luer-lock connector 3 is connected to the syringe outlet.
- the respective tubes 2 are then passed through the piercing station, and through rubber seals 4 of two waste blood holding vessels 5.
- Each of the respective syringes 1 is then-pierced through its side with a respective hypodermic needle 42, 43, connected to paraffin oil supplies in pressurised vessels 30 and 31 respectively.
- a pressure of 360 torr is applied to both pressure vessels 30 and 31, which causes paraffin oil to be displaced into the syringes 1 at a rate of approximately 0.1 m per minute.
- the inflowing paraffin oil prevent sedimentation of red cells in the blood, and displaces the blood through the tubing 2.
- the pressure at the pressure transducer 20 is observed, until it is steady, with a steady flow of blood entering vessel 5.
- the tubes 2 of both channels are then simultaneously pierced with the single needle 10, and the pressure at transducer 20 is observed further.
- a confirmatory check of bleeding through holes 12 is carried out noting the signal received at the silicon photodiode. Bleeding from holes 12 causes the signal to be much reduced, so that on-set and cessation of bleeding can be noted and confirmed.
- FIG. 4 illustrates a typical pressure trace obtained for channels I and II of two-channel apparatus.
- FIG. 4 the trace shown for channel II illustrates the normal process of haemostatis and clotting, when no anticoagulant is used.
- Point A is FIG. 4 represents the point at which the tubes 2 are pierced, and as can be seen, the pressure in vessel 5 descreased rapidly, and then slowly rises over a period of approximately two minutes, as haemostatic plugs are formed in holes 12. The pressure in channel II then rises again to its original level of 60 torr, until clotting occurs in tube 2. The on-set of clotting can be seen at point B, and clotting is complete at point C.
- an anticoagulant is introduced into the blood in columnar container 1.
- this is carried out by introducing into the paraffin oil flowing into the syringe 1 an amount of heparin such as to give a final concentration of 5 U/ml in the blood.
- the blood in channel I does not clot, but continues to flow in the tube.
- the valve 22 is closed, and valve 32 is operated, so as to reduce the pressure applied to pressure vessel 30 to 60 torr.
- the breakdown of the haemostatic plugs is shown not only by pressure drop at point E in FIG. 4, but also by the silicon photodiode referred to above.
- the on-set of bleeding, as sensed by the photodiode, at point A is used to start a electronic clock, when blood appearing in the light pathway reaches a pre-set sensitivity threshold, and decreases the photodiode output below that threshold stops the Quartz clock, to show the elapsed (thrombolysis) time.
- the arrangement is generally the same as illustrated in FIG. 1, except that it is not necessary to utilise the needle 10 to punch the tube 2.
- FIGS. 5A and 5B illustrates, a short piece of collagen fiber (surgical catgut), having a diameter of approximately 0.15 mm is placed within the tube 2, before the blood supply is started. Platelets adhere and aggregate on the surface of the catgut, as illustrated in FIG. 5A, and eventually occlude the tube. The rate and extent of the decline of the pressure in the vessel 5 indicate the platelet adhesion to the collagen, and subsequent thrombus formation.
- surgical catgut a short piece of collagen fiber having a diameter of approximately 0.15 mm is placed within the tube 2, before the blood supply is started. Platelets adhere and aggregate on the surface of the catgut, as illustrated in FIG. 5A, and eventually occlude the tube. The rate and extent of the decline of the pressure in the vessel 5 indicate the platelet adhesion to the collagen, and subsequent thrombus formation.
- This procedure allows the quantative measurement of platelet function which is most characteristically changed in certain disorders (for example Von Willebrand disease, and by drugs, for example aspirin).
- apparatus for the determination of the effects of collagen and the like on thrombus formation may omit the punching means 12. It is preferred however that apparatus in accordance with the invention comprises three substantially identical channels, all as illustrated in FIG. 1. The tubes 2 of two of the channels pass through the punching station, but the other does not, and is intended to receive the piece of collagen fiber.
- the invention also provides methods for the determination of clotting, haemostatis and thrombolysis factors of blood, using apparatus as described above.
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Abstract
Description
Claims (8)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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US09/078,506 US6004819A (en) | 1996-11-04 | 1998-05-14 | Blood testing device |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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US08/743,911 US5925569A (en) | 1986-09-10 | 1996-11-04 | Blood testing device and method |
US09/078,506 US6004819A (en) | 1996-11-04 | 1998-05-14 | Blood testing device |
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US08/743,911 Division US5925569A (en) | 1986-09-10 | 1996-11-04 | Blood testing device and method |
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US6004819A true US6004819A (en) | 1999-12-21 |
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US09/078,506 Expired - Fee Related US6004819A (en) | 1996-11-04 | 1998-05-14 | Blood testing device |
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Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2001055715A2 (en) * | 2000-01-25 | 2001-08-02 | Goltz Volker Freiherr Von | Device and method for detecting the coagulation functions of global, especially primary hemostasis |
US20050196748A1 (en) * | 2002-09-10 | 2005-09-08 | Placor, Inc. | Method and device for monitoring platelet function |
US20060269978A1 (en) * | 2005-04-25 | 2006-11-30 | Haworth William S | Method and device for monitoring platelet function |
US20080103397A1 (en) * | 2006-10-26 | 2008-05-01 | Jacob Barak | System and method for deep vein thrombosis prevention and diagnosis |
US7399637B2 (en) | 2004-04-19 | 2008-07-15 | Medtronic, Inc. | Blood coagulation test cartridge, system, and method |
US7422905B2 (en) | 2004-02-27 | 2008-09-09 | Medtronic, Inc. | Blood coagulation test cartridge, system, and method |
US7439069B2 (en) | 2004-02-27 | 2008-10-21 | Nippoldt Douglas D | Blood coagulation test cartridge, system, and method |
US20100099130A1 (en) * | 2006-10-25 | 2010-04-22 | Placor Inc. | Methods and devices for monitoring platelet function |
US10788502B2 (en) * | 2014-02-06 | 2020-09-29 | Fujimori Kogyo Co., Ltd. | Erythrocyte sedimentation inhibitor |
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Cited By (22)
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US7223365B2 (en) | 2000-01-25 | 2007-05-29 | Volker Freiherr Von Der Goltz | Device and method for detecting the coagulation functions of global, especially primary hemostasis |
DE10003093A1 (en) * | 2000-01-25 | 2001-08-02 | Goltz Volker Freiherr Von | Device and method for recording coagulation functions of global, especially primary, hemostasis |
WO2001055715A3 (en) * | 2000-01-25 | 2002-03-14 | Goltz Volker Freiherr Von | Device and method for detecting the coagulation functions of global, especially primary hemostasis |
DE10003093C2 (en) * | 2000-01-25 | 2002-05-16 | Goltz Volker Freiherr Von | Device for investigating properties of the global hemostasis function in whole blood or platelet-rich plasma |
US20030130596A1 (en) * | 2000-01-25 | 2003-07-10 | Von Der Goltz Volker Freiherr | Device and method for detecting the coagulation functions of global, especially primary hemostasis |
EP1471353A2 (en) * | 2000-01-25 | 2004-10-27 | Freiherr von der Goltz, Volker | Device and method for detecting the coagulation functions of global, especially primary hemostasis |
EP1471353A3 (en) * | 2000-01-25 | 2005-08-17 | Freiherr von der Goltz, Volker | Device and method for detecting the coagulation functions of global, especially primary hemostasis |
WO2001055715A2 (en) * | 2000-01-25 | 2001-08-02 | Goltz Volker Freiherr Von | Device and method for detecting the coagulation functions of global, especially primary hemostasis |
US7309607B2 (en) | 2002-09-10 | 2007-12-18 | Placor Inc. | Method and device for monitoring platelet function |
US20050196748A1 (en) * | 2002-09-10 | 2005-09-08 | Placor, Inc. | Method and device for monitoring platelet function |
US20090203064A1 (en) * | 2002-09-10 | 2009-08-13 | Placor Inc. | Method and device for monitoring platelet function |
US7534620B2 (en) | 2002-09-10 | 2009-05-19 | Placor Inc. | Method and device for monitoring platelet function |
US7439069B2 (en) | 2004-02-27 | 2008-10-21 | Nippoldt Douglas D | Blood coagulation test cartridge, system, and method |
US7422905B2 (en) | 2004-02-27 | 2008-09-09 | Medtronic, Inc. | Blood coagulation test cartridge, system, and method |
US7399637B2 (en) | 2004-04-19 | 2008-07-15 | Medtronic, Inc. | Blood coagulation test cartridge, system, and method |
US20060269978A1 (en) * | 2005-04-25 | 2006-11-30 | Haworth William S | Method and device for monitoring platelet function |
US20100099130A1 (en) * | 2006-10-25 | 2010-04-22 | Placor Inc. | Methods and devices for monitoring platelet function |
US20080103397A1 (en) * | 2006-10-26 | 2008-05-01 | Jacob Barak | System and method for deep vein thrombosis prevention and diagnosis |
US8597194B2 (en) * | 2006-10-26 | 2013-12-03 | Medical Compression Systems (Dbn) Ltd. | System and method for deep vein thrombosis prevention and diagnosis |
US9788738B2 (en) | 2006-10-26 | 2017-10-17 | Medical Compression Systems (Dbn) Ltd. | System and method for deep vein thrombosis prevention and diagnosis |
US20180035902A1 (en) * | 2006-10-26 | 2018-02-08 | Zimmer Dental Ltd. | System and method for deep vein thrombosis prevention and diagnosis |
US10788502B2 (en) * | 2014-02-06 | 2020-09-29 | Fujimori Kogyo Co., Ltd. | Erythrocyte sedimentation inhibitor |
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